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1155595-91-7

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1155595-91-7 Usage

General Description

1H-pyrazole-4-carboxaldehyde, 3,5-dimethyl-1-(2-propenyl)- is a chemical compound with the molecular formula C9H10N2O. It is a pyrazole derivative with a carboxaldehyde group and two methyl groups located at the 3 and 5 positions on the pyrazole ring. Additionally, it contains a 2-propenyl group attached to the carbon at position 1 of the pyrazole ring. 1H-pyrazole-4-carboxaldehyde, 3,5-dimethyl-1-(2-propenyl)- is commonly used as a building block in organic synthesis and is utilized in the production of various pharmaceuticals, agrochemicals, and other fine chemicals due to its versatile reactivity and functional groups. It may also exhibit biological activity and be used as a research tool in the development of new drugs and chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1155595-91-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,5,5,9 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1155595-91:
(9*1)+(8*1)+(7*5)+(6*5)+(5*5)+(4*9)+(3*5)+(2*9)+(1*1)=177
177 % 10 = 7
So 1155595-91-7 is a valid CAS Registry Number.

1155595-91-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-1-prop-2-enylpyrazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-ALLYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1155595-91-7 SDS

1155595-91-7Downstream Products

1155595-91-7Relevant articles and documents

2-(pyrazol-4-yl)-1,3-oxaselenolanes from pyrazole carbaldehydes and 2-selanyl-1-ethanol

Papernaya, Lyubov K.,Shatrova, Alexandra A.,Levanova, Ekaterina P.,Albanov, Alexandr I.,Klyba, Lyudmila V.,Rudyakova, Elena V.,Levkovskaya, Galina G.

, p. 5 - 11 (2015)

Pyrazole carbaldehydes react with 2-selanyl-1-ethanol at room temperature in the presence of trimethylchlorosilane followed by treatment C with triethyl amine to afford the corresponding 2-(pyrazol-4-yl)-1,3-oxaselenolanes. The structure of the novel compounds was confirmed by IR, 13 C, 1 H, 15N, and 77 Se NMR spectroscopy.this article online at wileyonlinelibrary.com.

Selenoacetalyzation of 4-formylpyrazoles in the presence of trimethylchlorosilane

Papernaya, Lyubov K.,Shatrova, Alexandra A.,Levanova, Ekaterina P.,Albanov, Alexandr I.,Klyba, Lyudmila V.,Rudyakova, Elena V.,Levkovskaya, Galina G.

, p. 466 - 475 (2013/12/04)

The reaction of 3,5-dimethyl-4-formylpyrazoles, bearing various substituents at N-1 atom, with propane-1,3-diselenol and 2-hydroxypropane-1,3- diselenol in the presence of Cyrillic capital letter teCyrillic capital letter emSCl proceeds without heating to

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